Labverity
Facility profile

Bieffe Medital S.p.A.

Testing & analysis · Drug product manufacturing · Sondrio 23035 · Italy

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed4 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisLabelManufacturePackSterilize
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Nov 17, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history9 inspection records

FDA inspection history

9 records, Oct 2009 – Nov 2023 · 2 NAI · 7 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 17, 2023VAIDrug Quality Assurance2024
Jun 28, 2019VAIDrug Quality Assurance2019
May 29, 2018VAIDrug Quality Assurance2018
Sep 22, 2015NAIDrug Quality Assurance2015
Aug 15, 2013VAICompliance: DevicesYes2013
Aug 15, 2013NAIPostmarket Assurance: DevicesYes2013
Aug 15, 2013VAIDrug Quality AssuranceYes2013
Oct 16, 2009VAIPostmarket Assurance: DevicesYes2010
Oct 16, 2009VAICompliance: DevicesYes2010

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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